Second Shift Collections Specialist

Abbott; Springfield (IL); Remote; USD 95,000 - 130,000; Full time

Job summary

Abbott is seeking a Field Clinical Specialist to support our Medical Affairs activities in Illinois. This is a remote role serving the Illinois region, with responsibilities spanning clinical trials coordination, protocol implementation, and data capture for Abbott products.

Expect up to 75% travel within the United States while maintaining strong collaboration with investigators and regulatory reporting. The role requires deep clinical expertise and ability to oversee trials from planning to

Job description

Field Clinical Specialist

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Career development with an international company where you can grow the career of which you dream.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

An excellent retirement savings plan with high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

We are seeking a Field Clinical Specialist to work Remotely covering

Illinois

for our Vascular division.

This is a remote role but candidate must live or relocate to Illinois.

The Field Clinical Specialist has comprehensive knowledge in the area of Medical Affairs. Ability to execute highly complex or specialized projects. As the Specialist in the Medical Affairs Sub-Function, considered as a highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Responsible for directing human clinical trials, phases III & IV for company products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.
• May participate in adverse event reporting and safety responsibilities monitoring.

Medical Device

Clinical Trial and/or Research Experience

80% Travel within the United States

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

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Medical & Scientific Affairs

DIVISION:

Remote

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 75 % of the Time

MEDICAL SURVEILLANCE:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

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